United States · FDA National Drug Code directory
amiodarone hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68382-298_b3f11ad6-9f3b-4054-9c51-3d2614c1002e
- Product NDC
- 68382-298
- Form
- TABLET
- Composition / generic term
- amiodarone hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230209
- Source listing expiry
- 20261231
Source-listed ingredients
- AMIODARONE HYDROCHLORIDE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (68382-298-06) · 68382-298-06
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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